Imaging single cells in a beam of live cyanobacteria with an X-ray laser (CXIDB ID 26)

doi:10.11577/1169686

Title: Imaging single cells in a beam of live cyanobacteria with an X-ray laser (CXIDB ID 26)

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Abstract

This entry contains ten diffraction patterns, and reconstructions images, of individual living Cyanobium gracile cells, imaged using 517 eV X-rays from the LCLS XFEL. The Hawk software package was used for phasing. The Uppsala aerosol injector was used for sample injection, assuring very low noise levels. The cells come from various stages of the cell cycle, and were imaged in random orientations.

Authors:: Schot, Gijs, vander

Publication Date:: Tue Feb 10 00:00:00 EST 2015

Other Number(s):: CXIDB ID 26

DOE Contract Number:: AC02-05CH11231

Research Org.:: Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Coherent X-ray Imaging Data Bank; Uppsala Univ. (Sweden)

Sponsoring Org.:: Uppsala University

Keywords:: XFEL; AMO; Single Particle X-ray Diffraction Imaging; X-ray Free-electorn Lasers; Cyanobium gracile; LCLS

OSTI Identifier:: 1169686

DOI:: https://doi.org/10.11577/1169686

Citation Formats


                    Schot, Gijs, vander. Imaging single cells in a beam of live cyanobacteria with an X-ray laser (CXIDB ID 26).  United States: N. p., 2015. 
        Web.  doi:10.11577/1169686.

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                    Schot, Gijs, vander. Imaging single cells in a beam of live cyanobacteria with an X-ray laser (CXIDB ID 26).  United States.  doi:https://doi.org/10.11577/1169686

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                    Schot, Gijs, vander. 2015.  
"Imaging single cells in a beam of live cyanobacteria with an X-ray laser (CXIDB ID 26)".  United States.  doi:https://doi.org/10.11577/1169686.  https://www.osti.gov/servlets/purl/1169686. Pub date:Tue Feb 10 00:00:00 EST 2015

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@article{osti_1169686,

  title        = {Imaging single cells in a beam of live cyanobacteria with an X-ray laser (CXIDB ID 26)},

  author       = {Schot, Gijs, vander},

  abstractNote = {This entry contains ten diffraction patterns, and reconstructions images, of individual living Cyanobium gracile cells, imaged using 517 eV X-rays from the LCLS XFEL. The Hawk software package was used for phasing. The Uppsala aerosol injector was used for sample injection, assuring very low noise levels. The cells come from various stages of the cell cycle, and were imaged in random orientations.},

  doi          = {10.11577/1169686},

  journal      = {},

  number       = ,

  volume       = ,

  place        = {United States},

  year         = {Tue Feb 10 00:00:00 EST 2015},

  month        = {Tue Feb 10 00:00:00 EST 2015}

}

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DOI: https://doi.org/10.11577/1169686

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